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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040959Generated: October 30, 2026

Diisopropylethylamine → HCID 66906271, compound

https://huagongshe.com/reaction/2040959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Bromo-2-chlorobenzothiazoleHCID 2049871—
Reactant(3S)-Piperidin-3-ol--hydrogen chloride (1/1)HCID 16211918—
SolventDimethylformamideHCID 6228—
ProductHCID 66906271HCID 66906271—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 6-bromo-2-chlorobenzo[d]thiazole (1.0 g, 4.0 mmol) and (S)-piperidin-3-ol hydrochloride (0.609 g, 4.43 mmol), and N,N-diisopropylethylamine (3.51 mL, 0.02012 mole) in N,N-dimethylformamide (2.0 mL) was heated to 150° C. under microwave irradiation for 15 minutes. The reaction mixture was transferred to a 100 mL round bottom flask (methanol rinse) and volatiles were removed under reduced pressure. The residue was partitioned between CHCl3 and saturated aqueous sodium carbonate. The organic layer was dried over MgSO4. Drying agent was removed by filtration and the filtrate was concentrated under reduced pressure. The crude material was purified by column chromatography on an Analogix IntelliFlash-280 (Analogix SF15-12 g, 100% CHCl3 to 60:40 CHCl3/ethyl acetate). Fractions containing product were combined and concentrated under reduced pressure to provide (S)-1-(6-bromobenzo[d]thiazol-2-yl)piperidin-3-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580968B2
Source datasetuspto-grants-2013_11
ORD IDord-b11c62f504ad446db12a33a16ab244c4
Source noteuspto-grants-2013_11